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Remote Capa Engineer Jobs (NOW HIRING)

This is a fixed hybrid role (onsite Tuesday-Thursyday & remote Mon/Fri) based in one of our ... Lead and manage corrective and preventive actions (CAPA) from investigation through effectiveness ...

This is a fixed hybrid role (onsite Tuesday-Thursyday & remote Mon/Fri) based in one of our ... Lead and manage corrective and preventive actions (CAPA) from investigation through effectiveness ...

This is a fixed hybrid role (onsite Tuesday-Thursyday & remote Mon/Fri) based in one of our ... Lead and manage corrective and preventive actions (CAPA) from investigation through effectiveness ...

This is a fixed hybrid role (onsite Tuesday-Thursyday & remote Mon/Fri) based in one of our ... Lead and manage corrective and preventive actions (CAPA) from investigation through effectiveness ...

This is a fixed hybrid role (onsite Tuesday-Thursyday & remote Mon/Fri) based in one of our ... Lead and manage corrective and preventive actions (CAPA) from investigation through effectiveness ...

This is a fixed hybrid role (onsite Tuesday-Thursyday & remote Mon/Fri) based in one of our ... Lead and manage corrective and preventive actions (CAPA) from investigation through effectiveness ...

PLM Developer

VA · Remote

$80K - $120K/yr

ORA_REMOTE Description SAIC is seeking a Digital Engineer PLM Associate (Digital Thread) to join our energized Solutions Technology Group Team of digital engineers to advance the ReadyOne Digital ...

Senior PLM Developer

VA · Remote

$120K - $160K/yr

Digital Engineer Schedule: Full-Time Shift: Day Job Travel: Yes - 25% of the time Minimum Clearance Required: None Clearance Level Must Be Able to Obtain: TS/SCI Potential for Remote Work: ORA_REMOTE ...

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Remote Capa Engineer information

See salary details

$38K

$115.9K

$191.5K

How much do remote capa engineer jobs pay per year?

As of Jun 19, 2026, the average yearly pay for remote capa engineer in the United States is $115,864.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $151,500.00 per year, depending on experience, location, and employer.

What is the difference between Remote Capa Engineer vs Remote Quality Engineer?

AspectRemote Capa EngineerRemote Quality Engineer
CredentialsISO 13485, FDA regulations, Six SigmaISO 9001, Six Sigma, QA certifications
Work EnvironmentMedical device, pharmaceutical, biotech industriesManufacturing, software, product development
Industry UsagePrimarily healthcare and biotech sectorsBroad across manufacturing, tech, and software
Common Search IntentRegulatory compliance, CAPA processes, medical device qualityProduct quality, testing, process improvement

Remote Capa Engineers focus on managing corrective and preventive actions in regulated industries like healthcare, ensuring compliance with standards such as ISO 13485. Remote Quality Engineers work across various sectors to improve product quality through testing and process improvements. While both roles emphasize quality management, the industry focus and specific certifications differ.

What are the key skills and qualifications needed to thrive as a Remote CAPA Engineer, and why are they important?

To thrive as a Remote CAPA (Corrective and Preventive Action) Engineer, you need a solid background in quality engineering, root cause analysis, and regulatory compliance, often supported by a degree in engineering or a related field. Familiarity with quality management systems (such as ISO 13485 or FDA 21 CFR Part 820), CAPA software, and data analysis tools is typically required. Strong attention to detail, problem-solving skills, and effective virtual communication set standout professionals apart. These skills ensure accurate issue resolution, regulatory adherence, and seamless collaboration in distributed work environments.

How does a Remote CAPA Engineer typically collaborate with cross-functional teams to resolve quality issues?

As a Remote CAPA (Corrective and Preventive Action) Engineer, you’ll regularly work with quality assurance, manufacturing, R&D, and regulatory teams to identify, investigate, and resolve quality concerns. Collaboration often involves virtual meetings, sharing documentation, and following up on action items remotely. Effective communication skills and a proactive approach are crucial for driving investigations, ensuring timely implementation of corrective actions, and verifying their effectiveness. Building strong relationships across departments helps streamline issue resolution and fosters a culture of continuous improvement, even in a remote work setting.

What is a Remote CAPA Engineer?

A Remote CAPA (Corrective and Preventive Action) Engineer is a professional responsible for identifying, investigating, and resolving quality issues within an organization, often working from a remote location. They analyze data, implement corrective and preventive measures, and ensure compliance with industry standards and regulations. Their work is crucial in maintaining product quality and safety, as well as continuous improvement in processes. Remote CAPA Engineers utilize digital tools and communication platforms to collaborate with cross-functional teams and document their findings.
More about Remote Capa Engineer jobs
What cities are hiring for Remote Capa Engineer jobs? Cities with the most Remote Capa Engineer job openings:
What are the most commonly searched types of Capa Engineer jobs? The most popular types of Capa Engineer jobs are:
What states have the most Remote Capa Engineer jobs? States with the most job openings for Remote Capa Engineer jobs include:
Infographic showing various Remote Capa Engineer job openings in the United States as of June 2026, with employment types broken down into 73% Full Time, 18% Part Time, and 9% Contract. Highlights an 100% Remote job distribution, with an average salary of $115,864 per year, or $55.7 per hour.
Quality Control Technician (Quality Engineer)

Quality Control Technician (Quality Engineer)

Ubertal Inc

Boca Raton, FL • Remote

Contractor

Posted 29 days ago


Job description

Job Title: Quality Control Technician (Quality Engineer – Contract)

Location: 100% Remote (Preferred Eastern or Central Time Zones)
Duration: 12 Months
Schedule: Full-Time, 40 Hours/Week | Standard Business Hours
Conversion: No FTE conversion available
Interview Process: 1 Round

We are seeking an experienced Quality Control Technician with strong validation and quality systems expertise to support documentation, statistical quality control, and regulatory compliance initiatives in a highly regulated pharmaceutical or manufacturing environment.

This role focuses on validation documentation, quality analysis, regulatory compliance, and cross-functional collaboration to ensure systems, products, and processes meet defined reliability and regulatory standards.

Key Responsibilities:

  • Write, review, approve, and execute validation documentation and technical reports for systems, products, and processes

  • Prepare validation protocols, test equipment, and evaluate validation data

  • Conduct statistical quality control analysis of testing results and process anomalies

  • Prepare reports summarizing study results and conformance to acceptance criteria

  • Support development and maintenance of validation programs and Standard Operating Procedures (SOPs)

  • Verify calibration, maintenance, and repair of instruments supporting Quality Systems validation

  • Participate in FMEA, RCA, and CAPA development activities

  • Ensure corrective and preventive measures meet reliability and compliance standards

  • Maintain working knowledge of FDA, CLIA, cGMP, Medical Device Directives, and other applicable regulatory standards

  • Support procedural document management and regulatory audit readiness

  • Communicate cross-functionally regarding validation studies and project deliverables

Required Qualifications:

  • Bachelor’s degree in Science, Engineering, or related field (or equivalent combination of education and relevant experience)

  • Minimum 3 years of quality/validation experience in pharmaceutical manufacturing or a highly regulated industry

  • Strong working knowledge of cGMP principles and regulatory compliance requirements

  • Experience writing and approving validation and technical documentation

  • Experience participating in FMEA, RCA, and CAPA processes

  • Strong analytical, critical thinking, and problem-solving skills

  • Project management skills with ability to manage multiple priorities and tight deadlines

  • Proficiency in Microsoft Office, statistical tools, and electronic quality systems

  • Strong written, verbal, and interpersonal communication skills

  • Ability to maintain confidentiality and demonstrate professional judgment

Preferred Qualifications:

  • ASQ Certification

  • Experience in medical device or regulated laboratory environments

This remote contract opportunity is ideal for a quality professional with deep validation experience, strong regulatory knowledge, and the ability to drive compliance and quality excellence within a regulated pharmaceutical or manufacturing environment.